DNA analysis discrete sequence variation panel   55208-3

LOINC Code


LOINC code55208-3
nameDNA analysis discrete sequence variation panel
descriptionThis panel contains terms used to report details associated with molecular genetics discrete sequence variation results.
statusACTIVE

Fully-Specified Name

componentDNA analysis discrete sequence variation panel
property-
timePt  =  Point in time:  To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements.
systemBld/Tiss
    Bld  =  Whole blood
    Tiss  =  Tissue, unspecified
scale-
methodMolgen  =  Molecular Genetics:  General class of methods used to detect genetic attributes on a molecular basis including RFL, PCR and other methods.

Additional Names

short nameDNA analysis discrete seq var Pnl

Basic Attributes

classPANEL.HL7.GENETICS
type1  Laboratory
order vs. observationOrder

Panel Components

48018-6Gene studied [ID]
48013-7Genomic reference sequence [ID]
51958-7Transcript reference sequence [ID]
48008-7Allele name [Identifier]
48003-8DNA sequence variation identifier [Identifier]
48004-6DNA change (c.HGVS)
48019-4DNA change type
48005-3Amino acid change (pHGVS)
48006-1Amino acid change [Type]
47999-8DNA region name [Identifier]
53034-5Allelic state
48002-0Genomic source class [Type]
47998-0DNA sequence variation display name [Text] Narrative
53037-8Genetic variation clinical significance [Imp]
53040-2Genetic variation's effect on drug metabolism
51961-1Genetic variation's effect on drug efficacy
69548-6Genetic variant assessment

Associated Observations

LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations.

Member of these Panels

55207-5Genetic analysis discrete result panel

History/Usage

first released
last updated2.56
last change typeMIN  - change to field other than name

Related Names

Blood
Deoxyribonucleic acid
DNA analysis discrete seq var Pnl
Genetic
Genetics
Genomic
Heredity
Heritable
HL7.GENETICS
Inherited
Molecular genetics
MOLPATH.GENERAL
Pan
PANEL.HL7.GENETICS
Panl
PCR
Pnl
Point in time
Positional Variant Panel
Random
Sequence Variant Panel
Tissue
Tissue, unspecified
WB
Whole blood
Whole blood or Tissue

Copyright © 2023 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2023, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

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